A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561902



Internal ID16349311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63395129..63426093hg38UCSC Ensembl
Innerchr13:63969262..64000226hg19UCSC Ensembl
Innerchr13:62867263..62898227hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3830965
hg1930965
hg1830965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3190n54
Supporting Variantsnssv812461
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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